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MODIFIED DDI SEROCARD TOXOPLASMA IGG TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K884249
510(k) Type
Traditional
Applicant
DISEASE DETECTION INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1989
Days to Decision
181 days

MODIFIED DDI SEROCARD TOXOPLASMA IGG TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K884249
510(k) Type
Traditional
Applicant
DISEASE DETECTION INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1989
Days to Decision
181 days